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As a key member of the Senior Leadership Team, you will work to build and lead a product transition team that is responsible for working to shape, improve, and guide the transfer of new Reagent products from R&D and/or current TPM into the Carlsbad GMP manufacturing environment as well as the improvement and scaling activities of current Reagent products.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Work as part of a team to execute GMP runs in close collaboration with Process Development and Quality. Assist with weighing of raw materials and electronic inventory transactions utilizing MES and/or Oracle.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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This position maintains systems to assure compliance regulatory and client requirements for all relevant GMP operations carried out within the organization for the manufacture of drug substances in compliance with FDA and international regulatory requirements for research, pre-clinical, clinical and commercial Active Pharmaceutical Ingredients (APIs.
$185,000 - $240,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Comply and enforce DOH regulations and HomeState GMP sanitation standards when performing cleaning tasks, preparing food, and serving beverages. Comply and enforce DOH regulations and HomeState GMP sanitation standards when performing cleaning tasks, preparing food, and serving beverages.
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Be able to schedule rooms, trainers, and resources and other required training (GMP, HR, EHS, etc. Knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, and cell culture products.
ExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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This individual will be required to accurately record information within documentation while maintaining strict adherence to FDA, GMP and ISO requirements. Normally receives instructions on routine work, detailed instructions for new assignments, provided by the Lead, Supervisor or Manger.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Follow GMP requirements and Quality Systems & Regulatory Compliance Department policies. Support the Quality Manager and Regulatory Manager in maintaining compliance with applicable regulations and standards, such as FDA, SQF, and customer requirements.
$47,133 a yearFull-timeExpandUpdated 2 days ago - UpvoteDownvoteShare Job
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Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements. Our buildings are modern, with employee accessible WiFi, dedicated break, quiet, and collaborative spaces, and an on-campus cafeteria.
ExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Strong understanding of regulatory requirements and guidelines, including FDA regulations (21 CFR Part 11, Part 210, Part 211), EU GMP Annex 15, and ICH guidelines. Develop and execute equipment validation protocols and reports for various types of pharmaceutical manufacturing equipment, including but not limited to packaging machinery, incubation chambers, and storage units.
Part-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Operate all material handling equipment in a safe manner+ Follow all standard operating procedures and GMP and SOX guidelines for all designated functions. Operate all material handling equipment in a safe manner+ Follow all standard operating procedures and GMP and SOX guidelines for all designated functions.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Previous experience interfacing with biologics drug product manufacturing sites and providing technical support during engineering runs/GMP operations is a plus. A basic understanding of formulation and drug product process development for biologics (antibodies, fusion proteins, bi-specifics, vaccines, antibody drug conjugates, etc.
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Strong knowledge and experience with size exclusion chromatography and FPLCs and well as strong understanding of GLP and GMP processes and documentation. Performing ion exchange chromatography, buffer and reagent preparation, FPLC (AKTA), HPLC, plate reader, etc.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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WORKING CONDITIONS: Our facilities are a heated, air-conditioned and humidity controlled production floor and /or clean room environment. Our campus is located on Lake Hazeltine with walking trails between buildings.
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Learn and participate in the company's lean manufacturing principles. Perform the set-up, calibration, testing and troubleshooting of reagent components and instruments. In this role you will formulate and test chemical and biological reagent products of varied complexity according to operational plans and customer demand.
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This Production Technician will perform a variety of assignments within a manufacturing environment. The Production Technician will be required to maintain up to date training records, support training of new employees and comply with all company policies and procedures.
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gmp job in Oceanside, CA
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